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Therapeutic Uses
Anti-Parkinsons
Storage Condition
Store at refrigerator (2-8ยฐC) for long term storage
Synonyms
Cabergoline EP Impurity B, 166533-36-4
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 95 %
Hazard Compound
No -Refer MSDS for accurate information
Cabergoline EP Impurity B is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
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Cabergoline EP Impurity B usage and description
Cabergoline EP Impurity B is a pharmacological impurity that is commonly used as a reference standard for the development and analysis of cabergoline-based drugs. Cabergoline is a dopamine agonist that is used for the treatment of hyperprolactinemia, a condition that occurs when there is an excess of prolactin hormone in the body. Cabergoline EP Impurity B is a chemical intermediate in the synthesis of cabergoline, and it is used to ensure quality control and batch-to-batch consistency of cabergoline-based drugs.
Chemically, Cabergoline EP Impurity B is known as 2-[(6-allylergolin-8ฮฒ-yl)carbonyl]-N,N-diethylglycinamide. It has a molecular weight of 466.6 g/mol and a molecular formula of C27H37N5O3. Cabergoline EP Impurity B is a white to off-white powder that is soluble in dimethylsulfoxide (DMSO) and dimethylformamide (DMF), and it is stable under normal storage conditions.
Cabergoline EP Impurity B is typically used in analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) to determine the purity, identity, and concentration of cabergoline-based drugs. It is also used as a reference standard for the development of new cabergoline-based drugs and for the validation of analytical methods for the quality control of these drugs.
Overall, Cabergoline EP Impurity B plays a critical role in ensuring the safety and effectiveness of cabergoline-based drugs and in advancing the field of pharmacology.